Variant report

Variant	rs9322003
Chromosome Location	chr6:145214982-145214983
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:145213043..145215099-chr6:145218450..145220487,2	K562	blood:

Extended variants
information (count: 84 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:82)

rs_ID	r²[population]
rs11969748	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12174209	0.87[EUR][1000 genomes]
rs13198108	0.84[ASN][1000 genomes]
rs13201654	0.84[ASN][1000 genomes]
rs13210332	0.96[EUR][1000 genomes]
rs13210889	0.80[ASN][1000 genomes]
rs13217690	0.83[ASN][1000 genomes]
rs1338696	0.82[ASN][1000 genomes]
rs1338697	0.82[ASN][1000 genomes]
rs1538401	0.84[ASN][1000 genomes]
rs1538402	0.84[ASN][1000 genomes]
rs2153108	0.84[ASN][1000 genomes]
rs2153109	0.84[ASN][1000 genomes]
rs2185143	0.84[ASN][1000 genomes]
rs35285375	0.98[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35946718	0.98[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4323328	0.97[EUR][1000 genomes]
rs4331996	0.84[ASN][1000 genomes]
rs4331997	0.84[ASN][1000 genomes]
rs4487599	1.00[EUR][1000 genomes]
rs4637659	0.84[ASN][1000 genomes]
rs4896761	0.84[ASN][1000 genomes]
rs57337295	0.98[EUR][1000 genomes]
rs57590687	0.81[ASN][1000 genomes]
rs6570656	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6909971	0.84[ASN][1000 genomes]
rs6910398	0.84[ASN][1000 genomes]
rs6913165	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6914560	0.84[ASN][1000 genomes]
rs6934724	0.83[ASN][1000 genomes]
rs6935054	0.81[ASN][1000 genomes]
rs6935093	0.84[ASN][1000 genomes]
rs6935178	0.84[ASN][1000 genomes]
rs71547172	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7742815	0.90[ASN][1000 genomes]
rs7742893	0.90[ASN][1000 genomes]
rs7743204	0.90[ASN][1000 genomes]
rs7762951	0.90[ASN][1000 genomes]
rs7769065	1.00[EUR][1000 genomes]
rs9285505	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9321999	0.80[ASN][1000 genomes]
rs9322000	0.84[ASN][1000 genomes]
rs9322001	0.84[ASN][1000 genomes]
rs9322002	0.84[ASN][1000 genomes]
rs9322004	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9322005	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9373433	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9373434	0.99[EUR][1000 genomes]
rs9376869	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9376873	0.82[ASN][1000 genomes]
rs9376874	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9386088	0.84[ASN][1000 genomes]
rs9386089	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9390243	0.90[EUR][1000 genomes]
rs9390249	0.83[ASN][1000 genomes]
rs9390250	0.83[ASN][1000 genomes]
rs9390251	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9390252	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9390253	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9390254	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9390257	0.99[EUR][1000 genomes]
rs9399514	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9399516	0.83[ASN][1000 genomes]
rs9399519	1.00[EUR][1000 genomes]
rs9399520	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9403621	0.95[EUR][1000 genomes]
rs9403622	0.87[ASN][1000 genomes]
rs9403625	0.83[ASN][1000 genomes]
rs9403626	0.83[ASN][1000 genomes]
rs9403627	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9403628	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9403629	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9403631	1.00[EUR][1000 genomes]
rs9403633	0.99[EUR][1000 genomes]
rs9403634	0.98[EUR][1000 genomes]
rs9497118	0.84[ASN][1000 genomes]
rs9497120	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9497121	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9497132	0.88[EUR][1000 genomes]
rs9688347	0.81[ASN][1000 genomes]
rs9688355	0.84[ASN][1000 genomes]
rs9688729	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016747	chr6:144917411-145599874	Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	esv1850377	chr6:145199259-145319640	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:145210600-145217000	Weak transcription	Right Atrium	heart
2	chr6:145213800-145215200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr6:145214000-145215400	Weak transcription	Osteobl	bone
4	chr6:145214400-145216400	Enhancers	A549	lung
5	chr6:145214800-145218400	Weak transcription	Fetal Intestine Large	intestine

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